Akbay Nuriye, Lakowicz Joseph R, Ray Krishanu
Center for Fluorescence Spectroscopy, Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, 725 West Lombard Street, Baltimore, Maryland 21201, United States.
J Phys Chem C Nanomater Interfaces. 2012 May 17;116(19):10766-10773. doi: 10.1021/jp2122714. Epub 2012 Apr 23.
Previously reported studies indicate that aluminum nanostructured substrates can potentially find widespread use in metal-enhanced fluorescence (MEF) applications particularly in the UV or near-UV spectral region toward label-free detection of biomolecules. MEF largely depends on several factors, such as chemical nature, size, shape of the nanostructure and its distance from the fluorophore. A detailed understanding of the MEF and its distance-dependence are important for its potential application in biomedical sensing. Our goal is to utilize intrinsic protein fluorescence for label-free binding assays. This is made possible by the use of metallic nanostructures which provide localized excitation and enhanced fluorescence of UV fluorophores and will also provide a way to separate the surface-bound proteins from the bulk samples. We evaluated varied probe distances from plasmonic nanostructures by the well-established layer-by-layer (LbL) technique. The investigated proteins were adsorbed on different numbers of alternate layers of poly(styrene sulfonate) (PSS) and poly(allylamine hydrochloride) (PAH). Bovine serum albumin (BSA) was electrostatically attached to the positively charged PAH layer, and goat and rabbit IgG were attached to negatively charged PSS layer. We obtained a maximum of a ~ 9 fold increase in fluorescence intensity from BSA at a distance of ~9 nm from the Al nanostructured surface. Approximately 6- and 7- fold increases were observed from goat and rabbit IgG at a distance of ~8 nm, respectively. The minimum lifetimes were about 3-fold shorter than those on bare control quartz slides for all three proteins. The time-resolved intensity decays were analyzed with a lifetime distribution model to understand the distance effect on the metal-fluorophore interaction in detail. The present study indicates the distance dependence nature of metal-enhanced intrinsic fluorescence of proteins and potential of LbL assembly to control the metal-to-fluorophore distance in the UV wavelength region.
先前报道的研究表明,铝纳米结构基底在金属增强荧光(MEF)应用中具有广泛的潜在用途,特别是在紫外或近紫外光谱区域用于生物分子的无标记检测。MEF很大程度上取决于几个因素,如纳米结构的化学性质、尺寸、形状及其与荧光团的距离。深入了解MEF及其距离依赖性对于其在生物医学传感中的潜在应用至关重要。我们的目标是利用蛋白质固有荧光进行无标记结合分析。这通过使用金属纳米结构得以实现,金属纳米结构可提供局部激发并增强紫外荧光团的荧光,还将提供一种从大量样品中分离表面结合蛋白的方法。我们通过成熟的层层(LbL)技术评估了与等离子体纳米结构的不同探针距离。所研究的蛋白质吸附在不同层数的聚苯乙烯磺酸盐(PSS)和聚烯丙基胺盐酸盐(PAH)交替层上。牛血清白蛋白(BSA)通过静电作用附着于带正电荷的PAH层,山羊和兔免疫球蛋白(IgG)则附着于带负电荷的PSS层。在距铝纳米结构表面约9 nm的距离处,我们从BSA获得了荧光强度最大约9倍的增强。在距表面约8 nm的距离处,分别观察到山羊和兔IgG的荧光强度增强约6倍和7倍。对于所有三种蛋白质,其最短寿命比在裸露的对照石英载玻片上缩短了约3倍。用寿命分布模型分析时间分辨强度衰减,以详细了解距离对金属 - 荧光团相互作用的影响。本研究表明了蛋白质金属增强固有荧光的距离依赖性本质以及LbL组装在紫外波长区域控制金属与荧光团距离的潜力。